ePRO Resources

  1. Create Personalized Treatments With VR And RWD 5/13/2023

    Dive into the ways this cutting-edge technology is revolutionizing how healthcare providers create personalized treatment plans for patients suffering from chronic low back pain (CLBP).

  2. Overcoming Oncology Trial Challenges With ePRO Solutions 5/16/2023

    Discover effective strategies and solutions to overcome challenges in oncology studies and how to optimize trial design, patient recruitment, data management, and regulatory compliance.

  3. Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials 6/24/2024

    Willie Muehlhausen, Co-CEO and Founder of Safira Clinical Research, and Tim Davis, VP of Strategy at MyVeeva for Patients, discuss how ePRO delivery needs to change to better serve modern trials.

  4. C3 Summit Recap: Shaping The Future Of eCOA/ePRO Highlights 2/10/2022

    Understand how the rapid shift to decentralized clinical trials required pharma companies and CROs to adapt data capture techniques quickly while remaining compliant with local regulations.

  5. Still Using Paper Diaries To Capture PRO Data? Read This. 1/8/2024

    Access real-world examples of how electronic patient-reported outcome measures (PROMs) optimize data quality and reliability and improve the statistical power of trial data.

  6. FDA's Vision On PRO Collection For RWE 9/24/2024

    In this presentation, a distinguished panel of experts illuminates the crucial role of patient-reported outcomes (PROs) in shaping regulatory decisions and drug development strategies.

  7. The Future Of Clinical Trials Rests On A Unified CTMS Platform 8/1/2022

    Discover why a unified CTMS platform is the answer for managing both the clinical trial itself and the data it produces when it comes to poorly integrated clinical trial management systems (CTMS).

  8. Simplify Today. Transform For The Future. 10/25/2023

    Maximize efficiency today with a cloud-based user-friendly platform that seamlessly adapts to the future of phase 1-3 trials. Watch to see how Zelta can help.

  9. Nevro Eliminates Majority Of Source Data Verification With ePRO And EDC 2/23/2023

    Read how a global medical device company was able to unlock new efficiencies by implementing data collection via electronic patient-reported outcome assessments.

  10. Streamlining Trials: How To Upgrade From Paper To EDC 4/19/2023

    Electronic modes have been shown to improve data quality in clinical trials. Address how equivalency can be achieved when migrating PROs from paper to ePRO.